Back

EVS-EN ISO 15747:2011

Plastic containers for intravenous injections (ISO 15747:2010)

General information

Withdrawn from 15.03.2019
Base Documents
ISO 15747:2010; EN ISO 15747:2011
ICS Groups
11.040.20 Transfusion, infusion and injection equipment
Directives or regulations
None

Standard history

Status
Date
Type
Name
15.03.2019
Main
EVS-EN ISO 15747:2019
02.11.2011
Main
EVS-EN ISO 15747:2011
Main
EVS-EN ISO 15747:2010
This International Standard contains requirements that relate to the safe handling and the physical, chemical and biological testing of plastic containers for parenterals. This International Standard is applicable to plastic containers for parenterals having one or more chambers and having a total nominal capacity in the range of 50 ml to 5 000 ml such as film bags or blow-moulded plastic bottles for direct administration of infusion (injection) solutions.

Required fields are indicated with *

*
*
*
PDF
19.52 € incl tax
Paper
19.52 € incl tax
Browse standard from 2.44 € incl tax
Standard monitoring
English (PDF 275 KB)

Related products

Main

EVS-EN ISO 15747:2019

Plastic containers for intravenous injections (ISO 15747:2018)
Newest version Valid from 15.03.2019
Main

EVS-EN ISO 80369-1:2018

Small-bore connectors for liquids and gases in healthcare applications - Part 1: General requirements (ISO 80369-1:2018)
Newest version Valid from 03.12.2018
Main

EVS-EN 60601-2-24:2015

Medical electrical equipment - Part 2-24: Particular requirements for the basic safety and essential performance of infusion pumps and controllers
Newest version Valid from 08.06.2015
Main

EVS-EN 60601-2-40:2019

Medical electrical equipment - Part 2-40: Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment
Newest version Valid from 16.01.2019

Customers who bought this item also bought

Main

EVS-EN ISO 80369-7:2017

Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications (ISO 80369-7:2016, Corrected version 2016-12-01)
Withdrawn from 01.06.2021
Main

CEN/TS 16555-1:2013

Innovation Management - Part 1: Innovation Management System
Withdrawn from 01.02.2021
Main

EVS-EN ISO 10993-16:2017

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)
Newest version Valid from 18.12.2017
Main

ISO 14155:2011

Clinical investigation of medical devices for human subjects -- Good clinical practice
Withdrawn from 28.07.2020

Standards designation

EVS Estonian standard
EN European standard (published by an CEN or CENELEC)
EN ISO International standard adopted as an European standard
ISO International Organization for Standardization’s standard
IEC International Electrotechnical Commission’s standard
HD CENELEC’s harmonisation document
   
EVS-EN European standard implemented in Estonia
EVS-EN ISO International standard adopted in Europe and implemented in Estonia
EVS-EN ISO/IEC International standard/International electrotechnical standard adopted in Europe and implemented in Estonia
EVS-IEC International electrotechnical standard implemented in Estonia
EVS-ISO International standard implemented in Estonia
   
A, AMD amedment
+A a full standard plus the amendment
/A only amendment
COR, AC corrigendum
+COR a full standard plus the corrigendum
NA national annex
+NA a full standard plus the national annex
/NA only national annex
TS technical specification
TR technical report
CWA agreement, developed by a CEN or CENELEC
prEVS-EN (etc) draft standard
   
et the standard is in Estonian only
en the standard is in English only
et-en the standard is in Parallel text Estonian-English